HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404831Generated: November 1, 2026
Ethyl chloroformate → HCID 86700476, compound
https://huagongshe.com/reaction/1404831
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Bromo-2-fluoro-6-nitroaniline | HCID 2773381 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86700476 | HCID 86700476 | 43.5% |
Reaction Steps
To a stirred solution of 4-bromo-2-fluoro-6-nitroaniline (1) (0.500 g, 2.12 mmol, 1.00 equiv) in THF (20 mL) was added NaH (0.250 g, 6.40 mmol, 3.00 equiv) portion wise at 0° C. After being stirred for 1 h at RT, ethyl chloroformate (1.00 mL, 10.6 mmol, 5.00 equiv) was added drop wise to the reaction mixture at 0° C. The reaction mixture was heated under reflux temperature for 36 h. After consumption of the starting material (by TLC), the reaction was quenched with saturated NH4Cl solution and extracted with EtOAc (2×100 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to give crude; which was purified by silica gel column chromatography (EtOAc/Hexane 1:4) to furnish compound 2 (0.350 g, 43.0%) as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916133B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-833da824cf4540ae87b739e4a3667829 |
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| Source note | uspto-grants-2014_12 |
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